898388-99-3

Basic information

• Product Name: 1,4-Dioxino[2,3-g]quinoline-9-carboxaldehyde, 7-chloro-2,3-dihydro-
• Synonyms: 1,4-Dioxino[2,3-g]quinoline-9-carboxaldehyde, 7-chloro-2,3-dihydro-
• CAS NO: 898388-99-3
• Molecular Formula: C12H8ClNO3
• Molecular Weight: 0
• Mol File: 898388-99-3.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,4-Dioxino[2,3-g]quinoline-9-carboxaldehyde, 7-chloro-2,3-dihydro-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-Dioxino[2,3-g]quinoline-9-carboxaldehyde, 7-chloro-2,3-dihydro-(898388-99-3)
• EPA Substance Registry System: 1,4-Dioxino[2,3-g]quinoline-9-carboxaldehyde, 7-chloro-2,3-dihydro-(898388-99-3)

Safety Data

• Hazardous Substances Data: 898388-99-3(Hazardous Substances Data)

Usage

Chemical class

Quinoline derivatives

Explanation

The compound belongs to a group of chemical compounds derived from quinoline, a tricyclic aromatic compound.

Explanation

The compound has demonstrated potential in fighting infections, treating malaria, and combating cancer.

Explanation

The compound's pharmacological properties make it a promising candidate for the development of new drugs.

Explanation

The compound features a six-membered oxygen-containing ring (1,4-dioxane) fused to a quinoline ring, which is a tricyclic aromatic system.

Explanation

A carboxaldehyde functional group (-CHO) is present in the molecule, providing additional reactivity and potential for further chemical modifications.

Explanation

The presence of a chlorine atom at the 7th position of the quinoline ring contributes to the compound's specific chemical and biological properties.

Explanation

The compound has demonstrated potential effectiveness in laboratory and animal studies, which is an essential step before moving on to clinical trials in humans.

Explanation

Due to its unique structure and pharmacological properties, the compound may serve as a starting point for the design and synthesis of new drugs targeting various diseases.

Pharmacological properties

Antimicrobial, antimalarial, and anticancer activities

Drug development

Potential use in developing new therapeutic agents

Chemical structure

1,4-dioxane ring fused to a quinoline ring

Functional group

Carboxaldehyde group attached to the quinoline ring

Chlorine substitution

Chlorine atom in the 7th position of the quinoline ring

Preclinical studies

Shown promising results

Lead compound

Valuable for the development of new therapeutic agents